HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 46102Erstellt: 24. Oktober 2026
Benzyl Bromide → (1R,2S,4R,5S)-5-(Benzyloxy)bicyclo[2.2.1]heptan-2-ol
https://huagongshe.com/de/reaction/46102
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Benzyl Bromide | HCID 7498 | — |
| Edukt | Tetrahydrofuran | HCID 8028 | — |
| Edukt | Sodium Hydroxide | HCID 14798 | — |
| Edukt | 15-Crown-5 | HCID 36336 | — |
| Edukt | (1R,2S,4R,5S)-Bicyclo[2.2.1]heptane-2,5-diol | HCID 9989289 | — |
| Produkt | (1R,2S,4R,5S)-5-(Benzyloxy)bicyclo[2.2.1]heptan-2-ol | HCID 10036335 | — |
Reaktionsschritte
To a stirred solution of (1R,2S,4R,5S)-bicyclo[2.2.1]-heptane-2,5-diol (1.15 g, 8.97 mmol) and 15-crown-5 (0.054 mL, 0.269 mmol) in tetrahydrofuran (30.0 mL, 8.97 mmol) were added at 10° C. (ice/water bath) finely ground sodium hydroxide (2.15 g, 53.8 mmol) and 1-(bromomethyl)benzene (1.07 mL, 8.97 mmol). After stirring at 10° C. for 3 h, the mixture was stirred at ambient temperature overnight. The mixture was partitioned between EtOAc and water, and the organic portions were washed with brine, and conc. in vacuo. The crude product was purified by flash column chromatography (0 to 80% of ethyl acetate in hexanes). The title compound was obtained as a colorless oil.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08541592B2 |
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| Quelldatensatz | uspto-grants-2013_09 |
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| ORD ID | ord-0398e47c3d9a4f728465e8b40c186dab |
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| Quellennotiz | uspto-grants-2013_09 |
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